Memmi M - Search Results

1

Identification of a SCN5A founder mutation causing sudden death, Brugada syndrome, and conduction blocks in Southern Italy.

Curcio A, Malovini A, Mazzanti A, Memmi M, Gambelli P, La Rosa F, Bloise R, Indolfi C, Bellazzi R, Napolitano C. Curcio A, et al. Among authors: memmi m. Heart Rhythm. 2021 Oct;18(10):1698-1706. doi: 10.1016/j.hrthm.2021.07.003. Epub 2021 Jul 8. Heart Rhythm. 2021. PMID: 34245912

2

Brugada syndrome and sudden cardiac death in children.

Priori SG, Napolitano C, Giordano U, Collisani G, Memmi M. Priori SG, et al. Among authors: memmi m. Lancet. 2000 Mar 4;355(9206):808-9. doi: 10.1016/S0140-6736(99)05277-0. Lancet. 2000. PMID: 10711933

3

Mutations in the cardiac ryanodine receptor gene (hRyR2) underlie catecholaminergic polymorphic ventricular tachycardia.

Priori SG, Napolitano C, Tiso N, Memmi M, Vignati G, Bloise R, Sorrentino V, Danieli GA. Priori SG, et al. Among authors: memmi m. Circulation. 2001 Jan 16;103(2):196-200. doi: 10.1161/01.cir.103.2.196. Circulation. 2001. PMID: 11208676

4

Novel arrhythmogenic mechanism revealed by a long-QT syndrome mutation in the cardiac Na(+) channel.

Abriel H, Cabo C, Wehrens XH, Rivolta I, Motoike HK, Memmi M, Napolitano C, Priori SG, Kass RS. Abriel H, et al. Among authors: memmi m. Circ Res. 2001 Apr 13;88(7):740-5. doi: 10.1161/hh0701.089668. Circ Res. 2001. PMID: 11304498

5

Inherited Brugada and long QT-3 syndrome mutations of a single residue of the cardiac sodium channel confer distinct channel and clinical phenotypes.

Rivolta I, Abriel H, Tateyama M, Liu H, Memmi M, Vardas P, Napolitano C, Priori SG, Kass RS. Rivolta I, et al. Among authors: memmi m. J Biol Chem. 2001 Aug 17;276(33):30623-30. doi: 10.1074/jbc.M104471200. Epub 2001 Jun 15. J Biol Chem. 2001. PMID: 11410597 Free article.

6

Clinical and molecular characterization of patients with catecholaminergic polymorphic ventricular tachycardia.

Priori SG, Napolitano C, Memmi M, Colombi B, Drago F, Gasparini M, DeSimone L, Coltorti F, Bloise R, Keegan R, Cruz Filho FE, Vignati G, Benatar A, DeLogu A. Priori SG, et al. Among authors: memmi m. Circulation. 2002 Jul 2;106(1):69-74. doi: 10.1161/01.cir.0000020013.73106.d8. Circulation. 2002. PMID: 12093772

7

Long QT syndrome, Brugada syndrome, and conduction system disease are linked to a single sodium channel mutation.

Grant AO, Carboni MP, Neplioueva V, Starmer CF, Memmi M, Napolitano C, Priori S. Grant AO, et al. Among authors: memmi m. J Clin Invest. 2002 Oct;110(8):1201-9. doi: 10.1172/JCI15570. J Clin Invest. 2002. PMID: 12393856 Free PMC article.

8

FKBP12.6 deficiency and defective calcium release channel (ryanodine receptor) function linked to exercise-induced sudden cardiac death.

Wehrens XH, Lehnart SE, Huang F, Vest JA, Reiken SR, Mohler PJ, Sun J, Guatimosim S, Song LS, Rosemblit N, D'Armiento JM, Napolitano C, Memmi M, Priori SG, Lederer WJ, Marks AR. Wehrens XH, et al. Among authors: memmi m. Cell. 2003 Jun 27;113(7):829-40. doi: 10.1016/s0092-8674(03)00434-3. Cell. 2003. PMID: 12837242 Free article.

9

Arrhythmogenesis in catecholaminergic polymorphic ventricular tachycardia: insights from a RyR2 R4496C knock-in mouse model.

Liu N, Colombi B, Memmi M, Zissimopoulos S, Rizzi N, Negri S, Imbriani M, Napolitano C, Lai FA, Priori SG. Liu N, et al. Among authors: memmi m. Circ Res. 2006 Aug 4;99(3):292-8. doi: 10.1161/01.RES.0000235869.50747.e1. Epub 2006 Jul 6. Circ Res. 2006. PMID: 16825580

10

Clinical phenotype and functional characterization of CASQ2 mutations associated with catecholaminergic polymorphic ventricular tachycardia.

di Barletta MR, Viatchenko-Karpinski S, Nori A, Memmi M, Terentyev D, Turcato F, Valle G, Rizzi N, Napolitano C, Gyorke S, Volpe P, Priori SG. di Barletta MR, et al. Among authors: memmi m. Circulation. 2006 Sep 5;114(10):1012-9. doi: 10.1161/CIRCULATIONAHA.106.623793. Epub 2006 Aug 14. Circulation. 2006. PMID: 16908766

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